CA2204919C - Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation - Google Patents
Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation Download PDFInfo
- Publication number
- CA2204919C CA2204919C CA002204919A CA2204919A CA2204919C CA 2204919 C CA2204919 C CA 2204919C CA 002204919 A CA002204919 A CA 002204919A CA 2204919 A CA2204919 A CA 2204919A CA 2204919 C CA2204919 C CA 2204919C
- Authority
- CA
- Canada
- Prior art keywords
- formula
- radical
- polyorganosiloxane
- group
- polyorganosiloxanes
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Fee Related
Links
- 238000000034 method Methods 0.000 title claims description 35
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims abstract description 33
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 21
- 239000001257 hydrogen Substances 0.000 claims abstract description 20
- 238000006459 hydrosilylation reaction Methods 0.000 claims abstract description 16
- 239000000203 mixture Substances 0.000 claims abstract description 16
- 125000004469 siloxy group Chemical group [SiH3]O* 0.000 claims abstract description 15
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 14
- -1 olefin compound Chemical class 0.000 claims abstract description 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 9
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 9
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 7
- 239000010703 silicon Substances 0.000 claims abstract description 7
- 125000003118 aryl group Polymers 0.000 claims abstract description 6
- 229910010271 silicon carbide Inorganic materials 0.000 claims abstract description 6
- 229910018540 Si C Inorganic materials 0.000 claims abstract description 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims abstract description 3
- 125000005370 alkoxysilyl group Chemical group 0.000 claims abstract description 3
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 3
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims abstract description 3
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract 2
- 229920000570 polyether Polymers 0.000 claims abstract 2
- 239000003054 catalyst Substances 0.000 claims description 27
- 230000008569 process Effects 0.000 claims description 20
- 238000002360 preparation method Methods 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 16
- 239000003153 chemical reaction reagent Substances 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 13
- 229910052697 platinum Inorganic materials 0.000 claims description 13
- 239000002243 precursor Substances 0.000 claims description 10
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 9
- 150000001875 compounds Chemical class 0.000 claims description 8
- 229910052721 tungsten Inorganic materials 0.000 claims description 8
- 229910052727 yttrium Inorganic materials 0.000 claims description 8
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- 229930195733 hydrocarbon Natural products 0.000 claims description 7
- 125000004429 atom Chemical group 0.000 claims description 6
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 230000007246 mechanism Effects 0.000 claims description 5
- 239000012429 reaction media Substances 0.000 claims description 5
- 238000009833 condensation Methods 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 239000007810 chemical reaction solvent Substances 0.000 claims description 3
- 229920001577 copolymer Polymers 0.000 claims description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
- 150000002367 halogens Chemical class 0.000 claims description 3
- 229910052759 nickel Inorganic materials 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000002947 alkylene group Chemical group 0.000 claims description 2
- 150000008366 benzophenones Chemical class 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000003700 epoxy group Chemical group 0.000 claims description 2
- 125000006682 monohaloalkyl group Chemical group 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- 125000006684 polyhaloalkyl group Polymers 0.000 claims description 2
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052703 rhodium Inorganic materials 0.000 claims description 2
- 229910052707 ruthenium Inorganic materials 0.000 claims description 2
- 238000004381 surface treatment Methods 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims 3
- 230000005494 condensation Effects 0.000 claims 2
- 229910052723 transition metal Inorganic materials 0.000 claims 2
- 150000003624 transition metals Chemical class 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 1
- 125000005160 aryl oxy alkyl group Chemical group 0.000 claims 1
- 125000005375 organosiloxane group Chemical group 0.000 claims 1
- 239000007858 starting material Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 abstract description 3
- 238000006356 dehydrogenation reaction Methods 0.000 abstract description 3
- 238000006482 condensation reaction Methods 0.000 abstract 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 abstract 1
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 28
- 229910018557 Si O Inorganic materials 0.000 description 24
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Inorganic materials [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 20
- 238000006243 chemical reaction Methods 0.000 description 19
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 14
- 239000000047 product Substances 0.000 description 14
- 230000006870 function Effects 0.000 description 10
- 239000003921 oil Substances 0.000 description 9
- XAYDWGMOPRHLEP-UHFFFAOYSA-N 6-ethenyl-7-oxabicyclo[4.1.0]heptane Chemical compound C1CCCC2OC21C=C XAYDWGMOPRHLEP-UHFFFAOYSA-N 0.000 description 7
- 239000004593 Epoxy Substances 0.000 description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 6
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 5
- 238000007306 functionalization reaction Methods 0.000 description 5
- 239000002904 solvent Substances 0.000 description 5
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 4
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 150000001336 alkenes Chemical class 0.000 description 3
- 229920000620 organic polymer Polymers 0.000 description 3
- SDRZFSPCVYEJTP-UHFFFAOYSA-N 1-ethenylcyclohexene Chemical compound C=CC1=CCCCC1 SDRZFSPCVYEJTP-UHFFFAOYSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
- 238000006136 alcoholysis reaction Methods 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000000576 coating method Methods 0.000 description 2
- 238000004132 cross linking Methods 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- 239000013067 intermediate product Substances 0.000 description 2
- 125000003253 isopropoxy group Chemical group [H]C([H])([H])C([H])(O*)C([H])([H])[H] 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000005461 lubrication Methods 0.000 description 2
- 229910052751 metal Inorganic materials 0.000 description 2
- 239000002184 metal Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 238000006467 substitution reaction Methods 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- OHXAOPZTJOUYKM-UHFFFAOYSA-N 3-Chloro-2-methylpropene Chemical compound CC(=C)CCl OHXAOPZTJOUYKM-UHFFFAOYSA-N 0.000 description 1
- PHKJVUUMSPASRG-UHFFFAOYSA-N 4-[4-chloro-5-(2,6-dimethyl-8-pentan-3-ylimidazo[1,2-b]pyridazin-3-yl)-1,3-thiazol-2-yl]morpholine Chemical compound CC=1N=C2C(C(CC)CC)=CC(C)=NN2C=1C(=C(N=1)Cl)SC=1N1CCOCC1 PHKJVUUMSPASRG-UHFFFAOYSA-N 0.000 description 1
- 102100021752 Corticoliberin Human genes 0.000 description 1
- 101000895481 Homo sapiens Corticoliberin Proteins 0.000 description 1
- 239000002841 Lewis acid Substances 0.000 description 1
- 239000007868 Raney catalyst Substances 0.000 description 1
- 229910000564 Raney nickel Inorganic materials 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- 239000006229 carbon black Substances 0.000 description 1
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 1
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 229920001429 chelating resin Polymers 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 239000000084 colloidal system Substances 0.000 description 1
- 239000003431 cross linking reagent Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000000280 densification Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000007517 lewis acids Chemical class 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 229910001510 metal chloride Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 239000002808 molecular sieve Substances 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 229920006136 organohydrogenpolysiloxane Polymers 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 229920001843 polymethylhydrosiloxane Polymers 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- URGAHOPLAPQHLN-UHFFFAOYSA-N sodium aluminosilicate Chemical compound [Na+].[Al+3].[O-][Si]([O-])=O.[O-][Si]([O-])=O URGAHOPLAPQHLN-UHFFFAOYSA-N 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 239000002966 varnish Substances 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/06—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/48—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms
- C08G77/50—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule in which at least two but not all the silicon atoms are connected by linkages other than oxygen atoms by carbon linkages
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0838—Compounds with one or more Si-O-Si sequences
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/21—Cyclic compounds having at least one ring containing silicon, but no carbon in the ring
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/385—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing halogens
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/04—Polysiloxanes
- C08L83/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D183/00—Coating compositions based on macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon, with or without sulfur, nitrogen, oxygen, or carbon only; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
- C09D183/06—Polysiloxanes containing silicon bound to oxygen-containing groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Silicon Polymers (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR9414057A FR2727119B1 (fr) | 1994-11-18 | 1994-11-18 | Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation |
| FR94/14057 | 1994-11-18 | ||
| PCT/FR1995/001505 WO1996016126A1 (fr) | 1994-11-18 | 1995-11-15 | Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CA2204919A1 CA2204919A1 (fr) | 1996-05-30 |
| CA2204919C true CA2204919C (fr) | 2003-09-23 |
Family
ID=9469089
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002204919A Expired - Fee Related CA2204919C (fr) | 1994-11-18 | 1995-11-15 | Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US6359097B1 (ja) |
| EP (1) | EP0792323B1 (ja) |
| JP (1) | JP3086259B2 (ja) |
| KR (1) | KR970707238A (ja) |
| CN (1) | CN1094141C (ja) |
| AR (2) | AR000255A1 (ja) |
| AT (1) | ATE181348T1 (ja) |
| AU (1) | AU707848B2 (ja) |
| BR (1) | BR9510344A (ja) |
| CA (1) | CA2204919C (ja) |
| DE (1) | DE69510367T2 (ja) |
| DK (1) | DK0792323T3 (ja) |
| ES (1) | ES2133834T3 (ja) |
| FR (1) | FR2727119B1 (ja) |
| GR (1) | GR3030799T3 (ja) |
| IL (1) | IL116025A0 (ja) |
| MX (1) | MX9703560A (ja) |
| NO (1) | NO309820B1 (ja) |
| PL (1) | PL183136B1 (ja) |
| TR (1) | TR199501445A2 (ja) |
| WO (1) | WO1996016126A1 (ja) |
| ZA (1) | ZA959786B (ja) |
Families Citing this family (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2727119B1 (fr) * | 1994-11-18 | 1997-01-03 | Rhone Poulenc Chimie | Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation |
| FR2749850B1 (fr) * | 1996-06-12 | 1998-09-04 | Rhone Poulenc Chimie | Procede d'hydrosilylation avec des huiles silicones et des motifs contenant au moins un cycle hydrocarbone dans lequel est inclus un atome d'oxygene en presence d'une composition catalytique |
| US6472492B2 (en) | 1996-08-06 | 2002-10-29 | Rhodia Chimie | Process for the manufacture of multifunctional polyorganosiloxanes (POSs) by dehydrocondensation and hydrosilylation, and device for carrying out this process |
| FR2752239B1 (fr) * | 1996-08-06 | 1998-12-04 | Rhone Poulenc Chimie | Procede de fabrication de polyorganosiloxanes (pos) multifonctionnels, par deshydrogenocondensation et hydrosilylation, et dispositif pour la mise en oeuvre de ce procede |
| BR9815506A (pt) * | 1997-07-11 | 2000-10-31 | Rhodia Chimie Sa | Processo de preparação de poliorganossiloxanos, poliorganossiloxanos, utlização de uma quantidade eficaz de pelo menos um poliorganossiloxano, composções de elastÈmero(s) e artigos de elastÈmero(s) |
| FR2809111B1 (fr) | 2000-05-16 | 2004-04-16 | Rhodia Chimie Sa | Huile polyoganosiloxane lubrifiante, emulsion aqueuse en contenant, leur preparation et leur utilisation pour le demoulage de metaux |
| AU2003258246A1 (en) * | 2002-08-16 | 2004-03-03 | Dow Corning Corporation | Enzyme catalyzed organosilicon esters and amides |
| JP4727931B2 (ja) * | 2003-01-21 | 2011-07-20 | 関西ペイント株式会社 | 上塗り塗料組成物 |
| DE10312636A1 (de) * | 2003-03-21 | 2004-09-30 | Goldschmidt Ag | Verfahren zur Umsetzung von Polyorganosiloxanen |
| TWI345576B (en) * | 2003-11-07 | 2011-07-21 | Dow Corning Toray Silicone | Curable silicone composition and cured product thereof |
| US7332179B2 (en) | 2003-12-12 | 2008-02-19 | Kimberly-Clark Worldwide, Inc. | Tissue products comprising a cleansing composition |
| DE10359764A1 (de) * | 2003-12-19 | 2005-07-14 | Goldschmidt Ag | Polysiloxane mit über SiOC-Gruppen gebundenen (Meth)acrylsäureestergruppen, Verfahren zu deren Herstellung sowie deren Verwendung als strahlenhärtbare abhäsive Beschichtung |
| JP4801320B2 (ja) * | 2003-12-19 | 2011-10-26 | 東レ・ダウコーニング株式会社 | 付加反応硬化型オルガノポリシロキサン樹脂組成物 |
| WO2005063843A1 (ja) * | 2003-12-26 | 2005-07-14 | Dow Corning Toray Co., Ltd. | 硬化性シリコーン組成物およびその硬化物 |
| WO2006055231A1 (en) * | 2004-11-19 | 2006-05-26 | Dow Corning Corporation | Silicone composition and cured silicone resin |
| US7642395B2 (en) | 2004-12-28 | 2010-01-05 | Kimberly-Clark Worldwide, Inc. | Composition and wipe for reducing viscosity of viscoelastic bodily fluids |
| US20060140899A1 (en) * | 2004-12-28 | 2006-06-29 | Kimberly-Clark Worldwide, Inc. | Skin cleansing system comprising an anti-adherent formulation and a cationic compound |
| ATE404635T1 (de) * | 2006-02-20 | 2008-08-15 | Shinetsu Chemical Co | Hitzeerhärtbare silikonzusammensetzung |
| WO2008088523A1 (en) * | 2006-12-21 | 2008-07-24 | Dow Corning Corporation | Dual curing polymers and methods for their preparation and use |
| JP5350267B2 (ja) * | 2006-12-21 | 2013-11-27 | ダウ・コーニング・コーポレイション | デュアル硬化ポリマー、その調製方法およびその使用 |
| CN101260190B (zh) * | 2008-04-28 | 2011-04-27 | 华南理工大学 | 多官能度聚硅氧烷偶联剂及其制备方法 |
| US20150274970A1 (en) * | 2014-03-26 | 2015-10-01 | Wacker Chemical Corporation | Control of internal viscosity in in situ polymerized organopolysiloxane emulsions |
| EP3325557A1 (en) * | 2015-07-20 | 2018-05-30 | Momentive Performance Materials GmbH | Modified filler particles and silicone compositions comprising the same |
| DE102015222139A1 (de) | 2015-11-10 | 2017-05-11 | Wacker Chemie Ag | Verfahren zur Imprägnierung von Textilien mit Zusammensetzungen enthaltend Alkoxypolysiloxane |
| CN114573816B (zh) * | 2022-03-08 | 2022-11-04 | 浙江大学 | 一种环氧基mq硅树脂及其制备方法和应用 |
| CN115746305B (zh) * | 2022-11-17 | 2023-09-19 | 万华化学集团股份有限公司 | 一种苯基聚硅氧烷及其制备方法与应用 |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2647798B1 (fr) * | 1989-05-31 | 1991-09-13 | Rhone Poulenc Chimie | Dispersion aqueuse a base d'huiles silicones fonctionnalisees pouvant reticuler en un elastomere par elimination de l'eau |
| US5310842A (en) * | 1990-09-14 | 1994-05-10 | Shin-Etsu Chemical Co., Ltd. | Higher alkoxy-substituted organopolysiloxane |
| JPH0625615A (ja) * | 1992-04-07 | 1994-02-01 | Shin Etsu Chem Co Ltd | プライマー組成物 |
| US5280098A (en) * | 1992-09-30 | 1994-01-18 | Dow Corning Corporation | Epoxy-functional silicone resin |
| JPH07133351A (ja) * | 1993-11-08 | 1995-05-23 | Shin Etsu Chem Co Ltd | エポキシ変性シリコーンの製造方法 |
| FR2727119B1 (fr) * | 1994-11-18 | 1997-01-03 | Rhone Poulenc Chimie | Polyorganosiloxanes fonctionnalises et l'un de leurs procedes de preparation |
-
1994
- 1994-11-18 FR FR9414057A patent/FR2727119B1/fr not_active Expired - Fee Related
-
1995
- 1995-11-15 KR KR1019970703283A patent/KR970707238A/ko not_active Application Discontinuation
- 1995-11-15 MX MX9703560A patent/MX9703560A/es not_active IP Right Cessation
- 1995-11-15 CA CA002204919A patent/CA2204919C/fr not_active Expired - Fee Related
- 1995-11-15 ES ES95940318T patent/ES2133834T3/es not_active Expired - Lifetime
- 1995-11-15 DK DK95940318T patent/DK0792323T3/da active
- 1995-11-15 JP JP08516618A patent/JP3086259B2/ja not_active Expired - Fee Related
- 1995-11-15 BR BR9510344A patent/BR9510344A/pt not_active IP Right Cessation
- 1995-11-15 DE DE69510367T patent/DE69510367T2/de not_active Expired - Fee Related
- 1995-11-15 EP EP95940318A patent/EP0792323B1/fr not_active Expired - Lifetime
- 1995-11-15 WO PCT/FR1995/001505 patent/WO1996016126A1/fr not_active Application Discontinuation
- 1995-11-15 AU AU41806/96A patent/AU707848B2/en not_active Ceased
- 1995-11-15 CN CN95196291A patent/CN1094141C/zh not_active Expired - Fee Related
- 1995-11-15 PL PL95320261A patent/PL183136B1/pl unknown
- 1995-11-15 AT AT95940318T patent/ATE181348T1/de not_active IP Right Cessation
- 1995-11-16 IL IL11602595A patent/IL116025A0/xx unknown
- 1995-11-17 AR AR33427195A patent/AR000255A1/es unknown
- 1995-11-17 AR ARP950100205A patent/AR000255A3/es unknown
- 1995-11-17 TR TR95/01445A patent/TR199501445A2/xx unknown
- 1995-11-17 ZA ZA959786A patent/ZA959786B/xx unknown
-
1997
- 1997-05-16 NO NO972249A patent/NO309820B1/no unknown
-
1999
- 1999-07-20 GR GR990401887T patent/GR3030799T3/el unknown
-
2000
- 2000-02-23 US US09/510,801 patent/US6359097B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP3086259B2 (ja) | 2000-09-11 |
| PL183136B1 (pl) | 2002-05-31 |
| JPH10501022A (ja) | 1998-01-27 |
| CN1094141C (zh) | 2002-11-13 |
| DK0792323T3 (da) | 1999-11-22 |
| PL320261A1 (en) | 1997-09-15 |
| FR2727119A1 (fr) | 1996-05-24 |
| NO972249D0 (no) | 1997-05-16 |
| FR2727119B1 (fr) | 1997-01-03 |
| WO1996016126A1 (fr) | 1996-05-30 |
| AR000255A1 (es) | 1997-06-18 |
| IL116025A0 (en) | 1996-01-31 |
| US6359097B1 (en) | 2002-03-19 |
| EP0792323B1 (fr) | 1999-06-16 |
| CA2204919A1 (fr) | 1996-05-30 |
| AU707848B2 (en) | 1999-07-22 |
| CN1165533A (zh) | 1997-11-19 |
| ES2133834T3 (es) | 1999-09-16 |
| DE69510367D1 (de) | 1999-07-22 |
| DE69510367T2 (de) | 1999-11-18 |
| MX9703560A (es) | 1997-08-30 |
| GR3030799T3 (en) | 1999-11-30 |
| AR000255A3 (es) | 1997-06-18 |
| KR970707238A (ko) | 1997-12-01 |
| EP0792323A1 (fr) | 1997-09-03 |
| TR199501445A2 (tr) | 1996-06-21 |
| ATE181348T1 (de) | 1999-07-15 |
| NO972249L (no) | 1997-07-17 |
| ZA959786B (en) | 1996-05-29 |
| NO309820B1 (no) | 2001-04-02 |
| BR9510344A (pt) | 1998-06-02 |
| AU4180696A (en) | 1996-06-17 |
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